Canonical Allele Identifier: CA2466664385

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380944C= , CM000685.2:g.154380944C=	GRCh38
NC_000023.10:g.153609304C= , CM000685.1:g.153609304C=	GRCh37
NC_000023.9:g.153262498C=	NCBI36
NG_008677.1:g.11509C= , LRG_745:g.11509C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000117.3:c.512C= MANE Select	NP_000108.1:p.Ser171=
ENST00000369842.9:c.512C= MANE Select	ENSP00000358857.4:p.Ser171=
NM_000117.2:c.512C= , LRG_745t1:c.512C=	NP_000108.1:p.Ser171=
ENST00000369835.3:c.407C=	ENSP00000358850.3:p.Ser136=
ENST00000369842.8:c.512C=	ENSP00000358857.4:p.Ser171=
ENST00000428228.5:c.*417C=	ENSP00000401081.1:n.*417C=
ENST00000471965.1:n.301C=
ENST00000485261.1:n.781C=
ENST00000486738.5:n.949C=
ENST00000492448.1:n.495C=
ENST00000682114.1:c.512C=	ENSP00000507245.1:p.Ser171=
ENST00000682478.1:n.702C=
ENST00000683576.1:n.702C=
ENST00000683627.1:c.512C=	ENSP00000507533.1:p.Ser171=
ENST00000684082.1:c.469C=	ENSP00000508266.1:n.469C=
ENST00000684633.1:n.484C=
ENST00000684678.1:c.508C=	ENSP00000507059.1:n.508C=
XM_024452349.1:c.518C=	XP_024308117.1:p.Ser173=